美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
0832-5323-11	0832-5323	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190621	N/A	NDA	NDA019123	Upsher-Smith Laboratories, LLC	POTASSIUM CHLORIDE	750 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0832-5323-11)
0245-5315-01	0245-5315	HUMAN PRESCRIPTION DRUG	KLOR-CON	potassium chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190621	N/A	NDA	NDA019123	Upsher-Smith Laboratories, LLC	POTASSIUM CHLORIDE	600 mg/1	100 BLISTER PACK in 1 BLISTER PACK (0245-5315-01) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0245-5315-89)
0245-5316-11	0245-5316	HUMAN PRESCRIPTION DRUG	KLOR-CON	potassium chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190621	N/A	NDA	NDA019123	Upsher-Smith Laboratories, LLC	POTASSIUM CHLORIDE	750 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0245-5316-11)
0245-5316-15	0245-5316	HUMAN PRESCRIPTION DRUG	KLOR-CON	potassium chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190621	N/A	NDA	NDA019123	Upsher-Smith Laboratories, LLC	POTASSIUM CHLORIDE	750 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0245-5316-15)
0245-5315-11	0245-5315	HUMAN PRESCRIPTION DRUG	KLOR-CON	potassium chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190621	N/A	NDA	NDA019123	Upsher-Smith Laboratories, LLC	POTASSIUM CHLORIDE	600 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0245-5315-11)
0245-5315-15	0245-5315	HUMAN PRESCRIPTION DRUG	KLOR-CON	potassium chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190621	N/A	NDA	NDA019123	Upsher-Smith Laboratories, LLC	POTASSIUM CHLORIDE	600 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0245-5315-15)
0245-5316-01	0245-5316	HUMAN PRESCRIPTION DRUG	KLOR-CON	potassium chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190621	N/A	NDA	NDA019123	Upsher-Smith Laboratories, LLC	POTASSIUM CHLORIDE	750 mg/1	100 BLISTER PACK in 1 BLISTER PACK (0245-5316-01) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0245-5316-89)
51655-226-26	51655-226	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20221025	N/A	NDA	NDA019123	Northwind Pharmaceuticals, LLC	POTASSIUM CHLORIDE	750 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-226-26)
51655-226-52	51655-226	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20221025	N/A	NDA	NDA019123	Northwind Pharmaceuticals, LLC	POTASSIUM CHLORIDE	750 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-226-52)
42291-506-01	42291-506	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190621	N/A	NDA	NDA019123	AvKARE	POTASSIUM CHLORIDE	750 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42291-506-01)
42291-506-50	42291-506	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190621	N/A	NDA	NDA019123	AvKARE	POTASSIUM CHLORIDE	750 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42291-506-50)